FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

IMPLANTABLE PACING LEAD TINED #3390 &

K Number: K823448 · Decision Dec 3, 1982
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
49
Review Days
17

Basic Information

Device Name
IMPLANTABLE PACING LEAD TINED #3390 &
K Number
K823448
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Oscor Inc.
Date Received
November 16, 1982
Decision Date
December 3, 1982
Product Code
DTB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DTB Permanent Pacemaker Electrode

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K130633 INTRODUCER SETS, MODEL ADELANTE RADIAL
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K122960 STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO
K122958 DELIVERY SHEATH, MODEL ADELANTE BREEZEWAY
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